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The electrochemical doping/dedoping kinetics, and the organic electrochemical transistor (OECT) performance of a series of polythiophene homopolymers with ethylene glycol units in their side chains using both kosmotropic and chaotropic anion solutions were studied. We compare their performance to a reference polymer, the polythiophene derivative with diethylene glycol side chains, poly(3-{[2-(2-methoxyethoxy)ethoxy]methyl}thiophene-2,5-diyl) (P3MEEMT). We find larger OECT material figure of merit, μC *, where μ is the carrier mobility and C * is the volumetric capacitance, and faster doping kinetics with more oxygen atoms on the side chains, and if the oxygen atom is farther from the polythiophene backbone. Replacing the oxygen atom close to the polythiophene backbone with an alkyl unit increases the film π-stacking crystallinity (higher electronic conductivity in the undoped film) but sacrifices the available doping sites (lower volumetric capacitance C * in OECT). We show that this variation in C * is the dominant factor in changing the μC * product for this family of polymers. With more oxygen atoms on the side chain, or with the oxygen atom farther from the polymer backbone, we observe both more passive swelling and higher C *. In addition, we show that, compared to the doping speed, the dedoping speed, as measured via spectroelectrochemistry, is both generally faster and less dependent on ion species or side chain oxygen content. Last, through OECT, electrochemical impedance spectroscopy (EIS) and spectroelectrochemistry measurements, we show that the chaotropic anion PF 6 − facilitates higher doping levels, faster doping kinetics, and lower doping thresholds compared to the kosmotropic anion Cl − , although the exact differences depend on the polymer side chains. Our results highlight the importance of balancing μ and C * when designing molecular structures for OECT active layers. 

A major limitation for polymeric mixed ionic/electronic conductors (MIECs) is the trade-off between ionic and electronic conductivity; changes made that improve one typically hinder the other. In order to address this fundamental problem, this work provides insight into ways that we could improve one type of conduction without hindering the other. We investigated a common oligoethylene glycol side chain polymer by adjusting the oxygen atom content and position, providing structural insights for materials that better balanced the two conduction pathways. The investigated polymer series showed the prototypical conflict between ionic and electronic conduction for oxygen atom content, with increasing oxygen atom content increasing ionic conductivity, but decreasing electronic conductivity; however, by increasing the oxygen atom distance from the polymer backbone, both ionic and electronic conductivity could be improved. Following these rules, we show that poly(3-(methoxyethoxybutyl)thiophene), when blended with lithium bistrifluoromethanesulfonimide (LiTFSI), matches the ionic conductivity of a comparable MIEC [poly(3-(methoxyethoxyethoxymethyl)thiophene)], while simultaneously showing higher electronic conductivity, highlighting the potential of this design strategy. We also provide strategies for tuning the MIEC performance to fit a desired application, depending on if electronic, ionic, or balanced conduction is most important. These results have implications beyond just polythiophene-based MIECs, as these strategies for balancing backbone crystallization and coordinating group interconnectivity apply for all semicrystalline conjugated polymers.